HNF1B-associated renal and extra-renal disease-an expanding clinical spectrum
Clissold, Rhian L, Hamilton, Alexander J, Hattersley, Andrew T, Ellard, Sian, Bingham, Coralie
Published in Nature reviews. Nephrology (01.02.2015)
Published in Nature reviews. Nephrology (01.02.2015)
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Journal Article
Discovery of a novel dominant mutation in the REN gene after forty years of renal disease: a case report
Clissold, Rhian L, Clarke, Helen C, Spasic-Boskovic, Olivera, Brugger, Kim, Abbs, Stephen, Bingham, Coralie, Shaw-Smith, Charles
Published in BMC nephrology (12.07.2017)
Published in BMC nephrology (12.07.2017)
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Journal Article
Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder
Clissold, Rhian L., Shaw-Smith, Charles, Turnpenny, Peter, Bunce, Benjamin, Bockenhauer, Detlef, Kerecuk, Larissa, Waller, Simon, Bowman, Pamela, Ford, Tamsin, Ellard, Sian, Hattersley, Andrew T., Bingham, Coralie
Published in Kidney international (01.07.2016)
Published in Kidney international (01.07.2016)
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Journal Article
Sociodemographic, Psychologic Health, and Lifestyle Outcomes in Young Adults on Renal Replacement Therapy
Hamilton, Alexander J, Clissold, Rhian L, Inward, Carol D, Caskey, Fergus J, Ben-Shlomo, Yoav
Published in Clinical journal of the American Society of Nephrology (07.12.2017)
Published in Clinical journal of the American Society of Nephrology (07.12.2017)
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Journal Article
Familial interstitial nephritis: 42 years from case series to genetic diagnosis
Clissold, Rhian L, Bingham, Coralie, Shaw-Smith, Charles
Published in Clinical nephrology (01.06.2019)
Published in Clinical nephrology (01.06.2019)
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Journal Article
Young adults’ perspectives on living with kidney failure: a systematic review and thematic synthesis of qualitative studies
Bailey, Phillippa K, Hamilton, Alexander J, Clissold, Rhian L, Inward, Carol D, Caskey, Fergus J, Ben-Shlomo, Yoav, Owen-Smith, Amanda
Published in BMJ open (01.01.2018)
Published in BMJ open (01.01.2018)
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Journal Article
Comment on Dubois-Laforgue et al. Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1B ( HNF1B ) Molecular Defects. Diabetes Care 2017;40:1436-1443
Clissold, Rhian L, Harries, Lorna W, Ellard, Sian, Bingham, Coralie, Hattersley, Andrew T
Published in Diabetes care (01.01.2018)
Published in Diabetes care (01.01.2018)
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Journal Article
Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/ Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1B (HNF1B) Molecular Defects. Diabetes Care 2017;40:1436–1443
Clissold, Rhian L, Harries, Lorna W, Ellard, Sian, Bingham, Coralie, Hattersley, Andrew T
Published in Diabetes care (01.01.2018)
Published in Diabetes care (01.01.2018)
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Journal Article
Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic
Clissold, Rhian L, Fulford, Jon, Hudson, Michelle, Shields, Beverley M, McDonald, Timothy J, Ellard, Sian, Hattersley, Andrew T, Bingham, Coralie
Published in Clinical kidney journal (01.08.2018)
Published in Clinical kidney journal (01.08.2018)
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Journal Article
SP030HNF1B WHOLE-GENE DELETIONS ARE ASSOCIATED WITH AUTISTIC TRAITS
Clissold, Rhian L, Ellard, Sian, Hattersley, Andrew T, Bingham, Coralie
Published in Nephrology, dialysis, transplantation (01.05.2015)
Published in Nephrology, dialysis, transplantation (01.05.2015)
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Journal Article
Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1[beta]-associated renal disease and can be symptomatic
Clissold, Rhian L, Fulford, Jon, Hudson, Michelle, Shields, Beverley M, Mcdonald, Timothy J, Ellard, Sian, Hattersley, Andrew T, Bingham, Coralie
Published in Clinical kidney journal (01.08.2018)
Published in Clinical kidney journal (01.08.2018)
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Journal Article